异位妊娠与葡萄胎的罕见关联1例报告

Santos Alexandre Bobbio dos, Pancieri Barbara Gobetti, Rios Camila Correia, B. E. S. Leticia Lanna de, Musiello Rubens Bermudes, C. Antônio
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引用次数: 0

摘要

异位磨牙妊娠是一种罕见的事件,发生在每20,000-100,000次妊娠中。这种情况可以表现为完全或部分臼齿妊娠,异位部位可以像非臼齿异位妊娠一样变化。当磨牙妊娠表现为输卵管异位妊娠时,两种情况相关的风险,包括输卵管破裂和恶性肿瘤的进展,都是复杂的。由于影像学检查通常无法区分是磨牙还是非磨牙异位妊娠,最终诊断通常是通过手术标本的组织病理学检查得出的。虽然特定的组织学结果可以证实葡萄胎的诊断,但免疫组织化学对于区分完全和部分葡萄胎是必不可少的。虽然在大多数情况下,手术切除被认为是最终的治疗方法,但据估计,20%的磨牙妊娠患者可能会发展为妊娠滋养细胞瘤,因此需要针对风险进行随访。本报告描述了一例输卵管磨牙妊娠,包括临床、诊断和治疗方面的回顾,以及对这种罕见关联的特殊性的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Rare Association of Ectopic Pregnancy and Hydatidiform Mole: A Case Report
An ectopic molar pregnancy is a rare event, occurring in 1 in every 20,000–100,000 pregnancies. The condition may present as a complete or partial molar pregnancy and the ectopic site can vary as in a non-molar ectopic pregnancy. When a molar pregnancy presents as a tubal ectopic pregnancy, the risks related to both conditions, including tubal rupture and progress to malignancy, are compounded. The definitive diagnosis is normally reached by histopathology of the surgical specimen, since imaging tests are usually unable to differentiate between a molar and a non-molar ectopic pregnancy. While the specific histological findings may confirm the diagnosis of hydatidiform mole, immunohistochemistry is essential to differentiate between a complete and a partial molar pregnancy. Although in the majority of cases surgical resection is considered the definitive treatment, it is estimated that 20% of patients with a molar pregnancy may develop gestational trophoblastic neoplasia, hence requiring a risk-specific follow-up. This report describes a case of a tubal molar pregnancy and includes a review of clinical, diagnostic and therapeutic aspects, as well as a discussion on the particularities of this rare association.
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